GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Echinicola vietnamensis KMM 6221, DSM 17526

Align Spermidine/putrescine import ATP-binding protein PotA, component of The spermidine/putrescine uptake porter, PotABCD (characterized)
to candidate Echvi_2123 Echvi_2123 ABC-type spermidine/putrescine transport systems, ATPase components

Query= TCDB::Q97Q42
         (385 letters)



>FitnessBrowser__Cola:Echvi_2123
          Length = 318

 Score =  174 bits (440), Expect = 4e-48
 Identities = 108/345 (31%), Positives = 193/345 (55%), Gaps = 41/345 (11%)

Query: 6   IEFKNVSKVFEDSNTKVLKDINFELEEGKFYTLLGASGSGKSTILNIIAGLLDATTGDIM 65
           ++   VSK + D+ +  L+D + +++ G   +++G SGSGKS++L IIAGL   + G + 
Sbjct: 4   LKVSEVSKRY-DAGSLALEDFSLQVKRGGVVSMVGESGSGKSSLLRIIAGLEVQSAGVVH 62

Query: 66  LDGVRINDIPTNKR-----DVHTVFQSYALFPHMNVFENVAFPLRLRKIDKKEIEQRVAE 120
           L   +I + P  K      ++  + Q Y L+P+  V EN+A PL L   DK   ++R AE
Sbjct: 63  LGDQKILN-PAQKLVPGYDEIQLIHQEYKLYPNSTVEENIARPLLL--YDKAYQKERTAE 119

Query: 121 VLKMVQLEGYEKRSIRKLSGGQRQRVAIARAIINQPRVVLLDEPLSALDLKLRTDMQYEL 180
           +L+++ L  ++ +  R+LSGGQ+Q+VAI RA+  +P V+LLDEP S+LD   + D+  EL
Sbjct: 120 ILELLSLRAFKDKKPRQLSGGQQQKVAIGRALSIEPEVLLLDEPFSSLDAIQKRDLIEEL 179

Query: 181 RELQQRLGITFVFVTHDQEEALAMSDWIFVMNDGEIVQSGTPVDIYDEPINHFVATFIGE 240
           +E+   L +T +FVTHD ++AL MS+ + ++  G+++Q G   +++ +P + +VA   G 
Sbjct: 180 KEIFDALEVTVIFVTHDVDDALLMSEELLIIQKGKLLQQGNVREVFRKPASAYVARLFGY 239

Query: 241 SNILPGTMIEDYLVEFNGKRFEAVDGGMKPNEPVEVVIRPEDLRITLPEEGKLQVKVDTQ 300
            N++PG                            E  +RP +++IT   +  ++ +V  Q
Sbjct: 240 LNLIPGA--------------------------EEAYVRPSEVKIT--SKTSIKAEVVKQ 271

Query: 301 LFRGVHYEIIAYDELGNE--WMIHSTRKAI-VGEEIGLDFEPEDI 342
            F  +HY ++      +E  W +    +++ VG+E+ LD++ E +
Sbjct: 272 QFL-IHYNLLTVKLEDSELFWKVDDPSRSVNVGDEVFLDYQKEQL 315


Lambda     K      H
   0.318    0.138    0.386 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 295
Number of extensions: 19
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 385
Length of database: 318
Length adjustment: 29
Effective length of query: 356
Effective length of database: 289
Effective search space:   102884
Effective search space used:   102884
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory